Canonical Allele Identifier: CA1819427169
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633264A= , CM000670.2:g.129633264A= GRCh38
NC_000008.10:g.130645510A= , CM000670.1:g.130645510A= GRCh37
NC_000008.9:g.130714692A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46664T=